Evidence map›Paper›PMID 31591744›Full record

ArticleAnnals of neurology2019

T lymphocytes and cytotoxic astrocyte blebs correlate across autism brains.

Marcello M DiStasio, Ikue Nagakura, Monica J Nadler, Matthew P Anderson

Open access · greenAbstract read
In one paragraph

Article in Annals of neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 4 pooled it
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 4 syntheses or guidelines pooled it, 81 citations in OpenAlex.

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  12. Neuroinflammation and autism: what have we learned so far?International journal of developmental disabilities · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Marcello M DiStasioDepartment of Neurology and Pathology, Beth Israel Deaconess Medical Center, Boston, MA.
Ikue NagakuraDepartment of Neurology and Pathology, Beth Israel Deaconess Medical Center, Boston, MA.
Monica J NadlerDepartment of Neurology and Pathology, Beth Israel Deaconess Medical Center, Boston, MA.
Matthew P AndersonDepartment of Neurology and Pathology, Beth Israel Deaconess Medical Center, Boston, MA.ORCID 0000-0003-4602-1811
Beth Israel Deaconess Medical Center · USBoston Children's Hospital · US

Funding

SYNAPTIC MECHANISMS IN HIPPOCAMPAL EPILEPTOGENESISP30HD018655 · NICHD · CHILDREN'S HOSPITAL BOSTON · PI POMEROY, SCOTT LOREN · 1985 to 2015
$26.2M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
VTA VGluT2 Sociability Circuit in Genetic AutismR01MH112714 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SAPER, CLIFFORD B · 2018 to 2022
$2.2M
Neurobiology of Aggression Comorbidity in AutismR01MH114858 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SAPER, CLIFFORD B · 2017 to 2021
$2.2M
Autism SpeaksAutism Speaks/National Alliance for Autism ResearchBoston Children's Hospital Intellectual and Developmental Disabilities Research Center P30 HD18655Landreth FoundationNancy Lurie Marks Family FoundationNICHD NIH HHS P30 HD018655NICHD NIH HHS U54 HD090255NIH National Institute of Mental Health R01 NS08916NIH National Institute of Neurological Disorders and StrokeNIMH NIH HHS R01 MH112714NIMH NIH HHS R01 MH114858Simons FoundationSimons Foundation/Autism BrainNet FA#345171
6 · The paper itself

Abstract

objectiveAutism spectrum disorder (ASD) affects 1 in 59 children, yet except for rare genetic causes, the etiology in most ASD remains unknown. In the ASD brain, inflammatory cytokine and transcript profiling shows increased expression of genes encoding mediators of the innate immune response. We evaluated postmortem brain tissue for adaptive immune cells and immune cell-mediated cytotoxic damage that could drive this innate immune response in the ASD brain.

methodsStandard neuropathology diagnostic methods including histology and immunohistochemistry were extended with automated image segmentation to quantify identified pathologic features in the postmortem brains.

resultsWe report multifocal perivascular lymphocytic cuffs contain increased numbers of lymphocytes in ~65% of ASD compared to control brains in males and females, across all ages, in most brain regions, and in white and gray matter, and leptomeninges. CD3

interpretationThe findings suggest dysregulated cellular immunity damages astrocytes at foci along the CSF-brain barrier in ASD. ANN NEUROL 2019;86:885-898.

Indexed as

AstrocytesAutism Spectrum DisorderBrainT-LymphocytesAdolescentAdultAgedChildChild, PreschoolFemaleHumansMaleMiddle AgedTissue BanksYoung Adult

Identifiers

PMID31591744
PMCPMC7210715
OpenAlexW2980017147

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.